re-solve
Your health deserves more than an inconclusive result
Variant reinterpretation is now a reality. Thousands of new studies, updated
databases, new patients, and emerging patterns. RE-SOLVE connects your
variant to new scientific findings – because uncertainty has an expiration date.
THE RE-SOLVE SOLUTION
Re-Solve provides automated evidence tracking and expert clinical reclassification for VUS.
A VUS is an inconclusive result that requires continuous evidence surveillance. By applying international guidelines to track scientific updates, Re-Solve transforms static data into into actionable clinical insights.
Who Re-solve can Assist
Uncertainty is a common problem
Resolution is possible.
We help to transform uncertain results into clear, actionable guidance
through personalized solutions.
Patients
Discover the opportunities to reinterpret your inconclusive genetic testing results
Physicians
Receive guidance on patient care from clear genetic results.
Laboratories
Enhance lab performance through clear and actionable genetic data.
Partners
Drive innovation. Improve patient outcomes
how it works
Do you have an uncertain genetic result?
Re-Solve turns uncertainty into clear answers.
1
Collect
Variants of uncertain significance (VUS) will be collected and carefully reviewed before advancing in the workflow.
2
Monitor
A systematic process of monitoring will track variant updates, new scientific findings and clinical relevance over time.
3
Resolve
Clear reports collect and synthesize scientific evidences to support a new interpretation of the variant.
why choose re-solve
Transforming uncertainty into actionable genomic insight
- Scientifically grounded:
RE-SOLVE is built on validated scientific data.
Every re-evaluation follows international guidelines, trusted data sources, and continuously updated evidence,—ensuring every decision is rigorous and responsible.
- Standardized by design:
Variant reinterpretation demands systematic evaluation.
RE-SOLVE applies standardized, traceable workflows that support clinical governance, regulatory compliance, and consistent decision-making.
- Distinct by design:
RE-SOLVE is not a laboratory service or a static database.
It is a dedicated system built exclusively for long-term variant re-evaluation and structured clinical communication.
RE-sources
Explore the benefit of the variant reclassification.
Blog
Dive into our blog to explore key topics shaping precision medicine and clinical research.
Coming soon
Scientific Publications
Learn how systematic reinterpretation of variants drives more accurate diagnoses and better patient care.
Clinical cases
Learn from detailed case studies showcasing the impact of variant reinterpretation in precision medicine.
Coming soon